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5-Isoxazolepropanoic acid, b-hydroxy-a-methylene-3-phenyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

337355-83-6

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337355-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 337355-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,7,3,5 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 337355-83:
(8*3)+(7*3)+(6*7)+(5*3)+(4*5)+(3*5)+(2*8)+(1*3)=156
156 % 10 = 6
So 337355-83-6 is a valid CAS Registry Number.

337355-83-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[Hydroxy-(3-phenyl-isoxazol-5-yl)-methyl]-acrylic acid methyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:337355-83-6 SDS

337355-83-6Relevant academic research and scientific papers

Isoxazole-based derivatives from Baylis-Hillman chemistry: Assessment of preliminary hypolipidemic activity

Patra,Batra,Bhaduri,Khanna,Chander,Dikshit

, p. 2269 - 2276 (2003)

The synthesis of isoxazole-based derivatives utilizing Baylis-Hillman chemistry and results of their preliminary bioevaluation as hypolipidemic agents in triton model are described.

Baylis-Hillman reaction assisted parallel synthesis of 3,5-disubstituted isoxazoles and their in vivo bioevaluation as antithrombotic agents

Batra,Roy,Patra,Bhaduri,Surin,Raghavan,Sharma,Kapoor,Dikshit

, p. 2059 - 2077 (2007/10/03)

The solution-phase parallel synthesis involving reactions of Baylis-Hillman products of 3-substituted-5-isoxazolecarbaldehydes with nucleophiles and their in vivo antithrombotic evaluations are described along with the results of in vitro platelet aggregation inhibition assay of a few compounds. Results of the detailed evaluation of one of the compounds as an inhibitor of platelet aggregation are also presented.

5-Isoxazolecarboxaldehyde: A novel substrate for fast Baylis-Hillman reaction

Patra,Batra,Kundu,Joshi,Roy,Bhaduri

, p. 276 - 280 (2007/10/03)

3-Aryl-5-isoxazolecarboxaldehyde undergoes fast Baylis-Hillman reaction with a variety of activated alkenes to yield the corresponding adducts in excellent yields. Some of the Baylis-Hillman adducts reported herein have been subsequently modified to obtai

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